{{Rsnum
|rsid=121913094
|Chromosome=4
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=FGG
|position=154606767
|Gene_s=FGG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=134850
|rsnum=121913094
|variant=0010
}}{{ClinVar
|rsid=121913094
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=155527919
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FGG:2266
|GENE_NAME=FGG
|GENE_ID=2266
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.155527919T>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000017790.2; RCV000017791.26
|CLNDBN=FIBRINOGEN MILANO 1; Thrombophilia, dysfibrinogenemic
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134850.0010
|Disease=FIBRINOGEN MILANO 1; Thrombophilia
}}